Chapter 6 Diversity analysis
6.1 Alpha diversity
# Calculate Hill numbers
richness <- genome_counts_filt %>%
column_to_rownames(var = "genome") %>%
dplyr::select(where(~ !all(. == 0))) %>%
hilldiv(., q = 0) %>%
t() %>%
as.data.frame() %>%
dplyr::rename(richness = 1) %>%
rownames_to_column(var = "sample")
neutral <- genome_counts_filt %>%
column_to_rownames(var = "genome") %>%
dplyr::select(where(~ !all(. == 0))) %>%
hilldiv(., q = 1) %>%
t() %>%
as.data.frame() %>%
dplyr::rename(neutral = 1) %>%
rownames_to_column(var = "sample")
phylogenetic <- genome_counts_filt %>%
column_to_rownames(var = "genome") %>%
dplyr::select(where(~ !all(. == 0))) %>%
hilldiv(., q = 1, tree = genome_tree) %>%
t() %>%
as.data.frame() %>%
dplyr::rename(phylogenetic = 1) %>%
rownames_to_column(var = "sample")
# Aggregate basal GIFT into elements
dist <- genome_gifts %>%
to.elements(., GIFT_db) %>%
traits2dist(., method = "gower")
functional <- genome_counts_filt %>%
column_to_rownames(var = "genome") %>%
dplyr::select(where(~ !all(. == 0))) %>%
hilldiv(., q = 1, dist = dist) %>%
t() %>%
as.data.frame() %>%
dplyr::rename(functional = 1) %>%
rownames_to_column(var = "sample") %>%
mutate(functional = if_else(is.nan(functional), 1, functional))
# Merge all metrics
alpha_div <- richness %>%
full_join(neutral, by = join_by(sample == sample)) %>%
full_join(phylogenetic, by = join_by(sample == sample)) %>%
full_join(functional, by = join_by(sample == sample))6.1.1 Wild samples
alpha_div %>%
pivot_longer(-sample, names_to = "metric", values_to = "value") %>%
left_join(., sample_metadata, by = join_by(sample == Tube_code)) %>%
filter(time_point=="0_Wild") %>%
mutate(metric=factor(metric,levels=c("richness","neutral","phylogenetic","functional"))) %>%
ggplot(aes(y = value, x = Population, group=Population, color=Population, fill=Population)) +
geom_boxplot(outlier.shape = NA) +
geom_jitter(alpha=0.5) +
scale_color_manual(name="Population",
breaks=c("Cold_wet","Hot_dry"),
labels=c("Cold","Hot"),
values=c('#008080', "#d57d2c")) +
scale_fill_manual(name="Population",
breaks=c("Cold_wet","Hot_dry"),
labels=c("Cold","Hot"),
values=c('#00808050', "#d57d2c50")) +
facet_wrap(. ~ metric,scales = "free") +
coord_cartesian(xlim = c(1, NA)) +
stat_compare_means(size=3, label.x=.58) +
theme_classic() +
theme(
strip.background = element_blank(),
panel.grid.minor.x = element_line(size = .1, color = "grey"),
axis.title.x = element_blank(),
axis.title.y = element_text(size=10),
axis.text.x = element_text(angle = 45, hjust = 1),
# Increase plot size
plot.title = element_text(size = 10),
axis.text = element_text(size = 8),
axis.title = element_text(size = 8)
) +
ylab("Alpha diversity")6.1.2 Acclimation samples
alpha_div %>%
pivot_longer(-sample, names_to = "metric", values_to = "value") %>%
left_join(., sample_metadata, by = join_by(sample == Tube_code)) %>%
filter(time_point=="1_Acclimation") %>%
mutate(metric=factor(metric,levels=c("richness","neutral","phylogenetic","functional"))) %>%
ggplot(aes(y = value, x = Population, group=Population, color=Population, fill=Population)) +
geom_boxplot(outlier.shape = NA) +
geom_jitter(alpha=0.5) +
scale_color_manual(name="Population",
breaks=c("Cold_wet","Hot_dry"),
labels=c("Cold","Hot"),
values=c('#008080', "#d57d2c")) +
scale_fill_manual(name="Population",
breaks=c("Cold_wet","Hot_dry"),
labels=c("Cold","Hot"),
values=c('#00808050', "#d57d2c50")) +
facet_wrap(. ~ metric,scales = "free") +
coord_cartesian(xlim = c(1, NA)) +
stat_compare_means(size=3, label.x=.58) +
theme_classic() +
theme(
strip.background = element_blank(),
panel.grid.minor.x = element_line(size = .1, color = "grey"),
axis.title.x = element_blank(),
axis.title.y = element_text(size=10),
axis.text.x = element_text(angle = 45, hjust = 1),
# Increase plot size
plot.title = element_text(size = 10),
axis.text = element_text(size = 8),
axis.title = element_text(size = 8)
) +
ylab("Alpha diversity")6.1.3 Antibiotics samples
alpha_div %>%
pivot_longer(-sample, names_to = "metric", values_to = "value") %>%
left_join(., sample_metadata, by = join_by(sample == Tube_code)) %>%
filter(time_point=="2_Antibiotics") %>%
mutate(metric=factor(metric,levels=c("richness","neutral","phylogenetic","functional"))) %>%
ggplot(aes(y = value, x = Population, group=Population, color=Population, fill=Population)) +
geom_boxplot(outlier.shape = NA) +
geom_jitter(alpha=0.5) +
scale_color_manual(name="Population",
breaks=c("Cold_wet","Hot_dry"),
labels=c("Cold","Hot"),
values=c('#008080', "#d57d2c")) +
scale_fill_manual(name="Population",
breaks=c("Cold_wet","Hot_dry"),
labels=c("Cold","Hot"),
values=c('#00808050', "#d57d2c50")) +
facet_wrap(. ~ metric,scales = "free") +
coord_cartesian(xlim = c(1, NA)) +
stat_compare_means(size=3, label.x=.58) +
theme_classic() +
theme(
strip.background = element_blank(),
panel.grid.minor.x = element_line(size = .1, color = "grey"),
axis.title.x = element_blank(),
axis.title.y = element_text(size=10),
axis.text.x = element_text(angle = 45, hjust = 1),
# Increase plot size
plot.title = element_text(size = 10),
axis.text = element_text(size = 8),
axis.title = element_text(size = 8)
) +
ylab("Alpha diversity")6.1.4 Transplant_1 samples
alpha_div %>%
pivot_longer(-sample, names_to = "metric", values_to = "value") %>%
left_join(., sample_metadata, by = join_by(sample == Tube_code)) %>%
filter(time_point=="3_Transplant1") %>%
mutate(metric=factor(metric,levels=c("richness","neutral","phylogenetic","functional"))) %>%
ggplot(aes(y = value, x = type, group=type, color=type, fill=type)) +
geom_boxplot(outlier.shape = NA) +
geom_jitter(alpha=0.5) +
scale_color_manual(name="Type",
breaks=c("Control","Hot_control", "Treatment"),
labels=c("Cold-Cold","Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c", "#76b183")) +
scale_fill_manual(name="Type",
breaks=c("Control","Hot_control", "Treatment"),
labels=c("Cold-Cold","Hot-Hot", "Cold-Hot"),
values=c("#4477AA50","#d57d2c50","#76b18350")) +
facet_wrap(. ~ metric,scales = "free") +
coord_cartesian(xlim = c(1, NA)) +
stat_compare_means(size=3, label.x=.7) +
theme_classic() +
theme(
strip.background = element_blank(),
panel.grid.minor.x = element_line(size = .1, color = "grey"),
axis.title.x = element_blank(),
axis.title.y = element_text(size=10),
axis.text.x = element_text(angle = 45, hjust = 1),
# Increase plot size
plot.title = element_text(size = 10),
axis.text = element_text(size = 8),
axis.title = element_text(size = 8)
) +
ylab("Alpha diversity")6.1.5 Transplant_2 samples
alpha_div %>%
pivot_longer(-sample, names_to = "metric", values_to = "value") %>%
left_join(., sample_metadata, by = join_by(sample == Tube_code)) %>%
filter(time_point=="4_Transplant2") %>%
mutate(metric=factor(metric,levels=c("richness","neutral","phylogenetic","functional"))) %>%
ggplot(aes(y = value, x = type, group=type, color=type, fill=type)) +
geom_boxplot(outlier.shape = NA) +
geom_jitter(alpha=0.5) +
scale_color_manual(name="Type",
breaks=c("Control","Hot_control", "Treatment"),
labels=c("Cold-Cold","Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c", "#76b183")) +
scale_fill_manual(name="Type",
breaks=c("Control","Hot_control", "Treatment"),
labels=c("Cold-Cold","Hot-Hot", "Cold-Hot"),
values=c("#4477AA50","#d57d2c50","#76b18350")) +
facet_wrap(. ~ metric,scales = "free") +
coord_cartesian(xlim = c(1, NA)) +
stat_compare_means(size=3, label.x=.7) +
theme_classic() +
theme(
strip.background = element_blank(),
panel.grid.minor.x = element_line(size = .1, color = "grey"),
axis.title.x = element_blank(),
axis.title.y = element_text(size=10),
axis.text.x = element_text(angle = 45, hjust = 1),
# Increase plot size
plot.title = element_text(size = 10),
axis.text = element_text(size = 8),
axis.title = element_text(size = 8)
) +
ylab("Alpha diversity")6.1.6 Post-Transplant_1 samples
alpha_div %>%
pivot_longer(-sample, names_to = "metric", values_to = "value") %>%
left_join(., sample_metadata, by = join_by(sample == Tube_code)) %>%
filter(time_point=="5_Post-FMT1") %>%
mutate(metric=factor(metric,levels=c("richness","neutral","phylogenetic","functional"))) %>%
ggplot(aes(y = value, x = type, group=type, color=type, fill=type)) +
geom_boxplot(outlier.shape = NA) +
geom_jitter(alpha=0.5) +
scale_color_manual(name="Type",
breaks=c("Control","Hot_control", "Treatment"),
labels=c("Cold-Cold","Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c", "#76b183")) +
scale_fill_manual(name="Type",
breaks=c("Control","Hot_control", "Treatment"),
labels=c("Cold-Cold","Hot-Hot", "Cold-Hot"),
values=c("#4477AA50","#d57d2c50","#76b18350")) +
facet_wrap(. ~ metric,scales = "free") +
coord_cartesian(xlim = c(1, NA)) +
stat_compare_means(size=3, label.x=.7) +
theme_classic() +
theme(
strip.background = element_blank(),
panel.grid.minor.x = element_line(size = .1, color = "grey"),
axis.title.x = element_blank(),
axis.title.y = element_text(size=10),
axis.text.x = element_text(angle = 45, hjust = 1),
# Increase plot size
plot.title = element_text(size = 10),
axis.text = element_text(size = 8),
axis.title = element_text(size = 8)
) +
ylab("Alpha diversity")6.1.7 Post-Transplant_2 samples
alpha_div %>%
pivot_longer(-sample, names_to = "metric", values_to = "value") %>%
left_join(., sample_metadata, by = join_by(sample == Tube_code)) %>%
filter(time_point=="6_Post-FMT2") %>%
mutate(metric=factor(metric,levels=c("richness","neutral","phylogenetic","functional"))) %>%
ggplot(aes(y = value, x = type, group=type, color=type, fill=type)) +
geom_boxplot(outlier.shape = NA) +
geom_jitter(alpha=0.5) +
scale_color_manual(name="Type",
breaks=c("Control","Hot_control", "Treatment"),
labels=c("Cold-Cold","Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c", "#76b183")) +
scale_fill_manual(name="Type",
breaks=c("Control","Hot_control", "Treatment"),
labels=c("Cold-Cold","Hot-Hot", "Cold-Hot"),
values=c("#4477AA50","#d57d2c50","#76b18350")) +
facet_wrap(. ~ metric,scales = "free") +
coord_cartesian(xlim = c(1, NA)) +
stat_compare_means(size=3, label.x=.7) +
theme_classic() +
theme(
strip.background = element_blank(),
panel.grid.minor.x = element_line(size = .1, color = "grey"),
axis.title.x = element_blank(),
axis.title.y = element_text(size=10),
axis.text.x = element_text(angle = 45, hjust = 1),
# Increase plot size
plot.title = element_text(size = 10),
axis.text = element_text(size = 8),
axis.title = element_text(size = 8)
) +
ylab("Alpha diversity")6.2 Beta diversity
beta_q0n <- genome_counts_filt %>%
column_to_rownames(., "genome") %>%
hillpair(., q = 0)
beta_q1n <- genome_counts_filt %>%
column_to_rownames(., "genome") %>%
hillpair(., q = 1)
beta_q1p <- genome_counts_filt %>%
column_to_rownames(., "genome") %>%
hillpair(., q = 1, tree = genome_tree)
beta_q1f <- genome_counts_filt %>%
column_to_rownames(., "genome") %>%
hillpair(., q = 1, dist = dist)6.3 Permanovas
6.3.1 1. Are the wild populations similar?
6.3.1.1 Wild: P.muralis vs P.liolepis
wild <- meta %>%
filter(time_point == "0_Wild")
# Create a temporary modified version of genome_counts_filt
temp_genome_counts <- transform(genome_counts_filt, row.names = genome_counts_filt$genome)
temp_genome_counts$genome <- NULL
wild.counts <- temp_genome_counts[, which(colnames(temp_genome_counts) %in% rownames(wild))]
identical(sort(colnames(wild.counts)), sort(as.character(rownames(wild))))
wild_nmds <- sample_metadata %>%
filter(time_point == "0_Wild")6.3.1.3 Richness
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.000012 0.000012 0.0012 999 0.975
Residuals 25 0.257281 0.010291
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Podarcis_liolepis Podarcis_muralis
Podarcis_liolepis 0.979
Podarcis_muralis 0.97302
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 1.542719 | 0.2095041 | 6.625717 | 0.001 |
| Residual | 25 | 5.820951 | 0.7904959 | NA | NA |
| Total | 26 | 7.363669 | 1.0000000 | NA | NA |
6.3.1.4 Neutral
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.000048 0.0000476 0.0044 999 0.948
Residuals 25 0.270114 0.0108046
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Podarcis_liolepis Podarcis_muralis
Podarcis_liolepis 0.946
Podarcis_muralis 0.94763
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 1.918266 | 0.2608511 | 8.822682 | 0.001 |
| Residual | 25 | 5.435610 | 0.7391489 | NA | NA |
| Total | 26 | 7.353876 | 1.0000000 | NA | NA |
6.3.1.5 Phylogenetic
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.03585 0.035847 2.4912 999 0.135
Residuals 25 0.35973 0.014389
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Podarcis_liolepis Podarcis_muralis
Podarcis_liolepis 0.133
Podarcis_muralis 0.12705
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 0.3218613 | 0.2162815 | 6.899207 | 0.001 |
| Residual | 25 | 1.1662981 | 0.7837185 | NA | NA |
| Total | 26 | 1.4881594 | 1.0000000 | NA | NA |
6.3.1.6 Functional
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.018367 0.018367 1.5597 999 0.203
Residuals 25 0.294402 0.011776
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Podarcis_liolepis Podarcis_muralis
Podarcis_liolepis 0.209
Podarcis_muralis 0.22328
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 0.0858578 | 0.172879 | 5.225323 | 0.053 |
| Residual | 25 | 0.4107775 | 0.827121 | NA | NA |
| Total | 26 | 0.4966352 | 1.000000 | NA | NA |
beta_q0n_nmds_wild <- beta_div_richness_wild$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE, trace=FALSE) %>%
vegan::scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(wild_nmds, by = join_by(sample == Tube_code))
beta_q1n_nmds_wild <- beta_div_neutral_wild$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE, trace=FALSE) %>%
vegan::scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(wild_nmds, by = join_by(sample == Tube_code))
beta_q1p_nmds_wild <- beta_div_phylo_wild$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
vegan::scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(wild_nmds, by = join_by(sample == Tube_code))
beta_q1f_nmds_wild <- beta_div_func_wild$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
vegan::scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(wild_nmds, by = join_by(sample == Tube_code))6.3.2 2. Effect of acclimation
accli <- meta %>%
filter(time_point == "1_Acclimation")
# Create a temporary modified version of genome_counts_filt
temp_genome_counts <- transform(genome_counts_filt, row.names = genome_counts_filt$genome)
temp_genome_counts$genome <- NULL
accli.counts <- temp_genome_counts[, which(colnames(temp_genome_counts) %in% rownames(accli))]
identical(sort(colnames(accli.counts)), sort(as.character(rownames(accli))))
accli_nmds <- sample_metadata %>%
filter(time_point == "1_Acclimation")6.3.2.2 Richness
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.11796 0.117959 12.963 999 0.003 **
Residuals 25 0.22748 0.009099
---
Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Cold_wet Hot_dry
Cold_wet 0.002
Hot_dry 0.0013711
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| Population | 1 | 1.639807 | 0.179834 | 5.481634 | 0.001 |
| Residual | 25 | 7.478640 | 0.820166 | NA | NA |
| Total | 26 | 9.118447 | 1.000000 | NA | NA |
6.3.2.3 Neutral
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.07844 0.078443 5.2384 999 0.032 *
Residuals 25 0.37437 0.014975
---
Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Cold_wet Hot_dry
Cold_wet 0.029
Hot_dry 0.030815
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| Population | 1 | 1.947003 | 0.2306127 | 7.493387 | 0.001 |
| Residual | 25 | 6.495736 | 0.7693873 | NA | NA |
| Total | 26 | 8.442739 | 1.0000000 | NA | NA |
6.3.2.4 Phylogenetic
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.06739 0.067395 2.9532 999 0.104
Residuals 25 0.57052 0.022821
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Cold_wet Hot_dry
Cold_wet 0.095
Hot_dry 0.098068
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| Population | 1 | 0.2441653 | 0.1224638 | 3.488854 | 0.032 |
| Residual | 25 | 1.7496100 | 0.8775362 | NA | NA |
| Total | 26 | 1.9937754 | 1.0000000 | NA | NA |
6.3.2.5 Functional
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.02496 0.024955 0.6729 999 0.454
Residuals 25 0.92714 0.037085
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Cold_wet Hot_dry
Cold_wet 0.448
Hot_dry 0.41979
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| Population | 1 | 0.0279454 | 0.0248037 | 0.6358634 | 0.466 |
| Residual | 25 | 1.0987171 | 0.9751963 | NA | NA |
| Total | 26 | 1.1266624 | 1.0000000 | NA | NA |
beta_q0n_nmds_accli <- beta_div_richness_accli$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE, trace=FALSE) %>%
vegan::scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(accli_nmds, by = join_by(sample == Tube_code))
beta_q1n_nmds_accli <- beta_div_neutral_accli$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE, trace=FALSE) %>%
vegan::scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(accli_nmds, by = join_by(sample == Tube_code))
beta_q1p_nmds_accli <- beta_div_phylo_accli$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
vegan::scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(accli_nmds, by = join_by(sample == Tube_code))
beta_q1f_nmds_accli <- beta_div_func_accli$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
vegan::scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(accli_nmds, by = join_by(sample == Tube_code))6.3.3 3. Comparison between Wild and Acclimation
accli1 <- meta %>%
filter(time_point == "0_Wild" | time_point == "1_Acclimation")
temp_genome_counts <- transform(genome_counts_filt, row.names = genome_counts_filt$genome)
temp_genome_counts$genome <- NULL
accli1.counts <- temp_genome_counts[,which(colnames(temp_genome_counts) %in% rownames(accli1))]
identical(sort(colnames(accli1.counts)),sort(as.character(rownames(accli1))))
accli1_nmds <- sample_metadata %>%
filter(time_point == "0_Wild" | time_point == "1_Acclimation")6.3.3.1 Number of samples used
[1] 54
beta_div_richness_accli1<-hillpair(data=accli1.counts, q=0)
beta_div_neutral_accli1<-hillpair(data=accli1.counts, q=1)
beta_div_phylo_accli1<-hillpair(data=accli1.counts, q=1, tree=genome_tree)
beta_div_func_accli1<-hillpair(data=accli1.counts, q=1, dist=dist)6.3.3.1.1 Richness
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.05014 0.050145 6.2252 999 0.011 *
Residuals 52 0.41886 0.008055
---
Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
0_Wild 1_Acclimation
0_Wild 0.014
1_Acclimation 0.015808
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| time_point | 1 | 0.6172653 | 0.0360987 | 3.933397 | 0.001 |
| species | 1 | 2.8279677 | 0.1653842 | 18.020647 | 0.001 |
| individual | 25 | 9.5739861 | 0.5599025 | 2.440331 | 0.001 |
| Residual | 26 | 4.0801621 | 0.2386146 | NA | NA |
| Total | 53 | 17.0993812 | 1.0000000 | NA | NA |
6.3.3.1.2 Neutral
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.0199 0.0199035 2.1213 999 0.139
Residuals 52 0.4879 0.0093827
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
0_Wild 1_Acclimation
0_Wild 0.142
1_Acclimation 0.15128
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| time_point | 1 | 0.9050519 | 0.0541893 | 6.651487 | 0.001 |
| species | 1 | 3.3236300 | 0.1989999 | 24.426315 | 0.001 |
| individual | 25 | 8.9352276 | 0.5349902 | 2.626702 | 0.001 |
| Residual | 26 | 3.5377576 | 0.2118206 | NA | NA |
| Total | 53 | 16.7016671 | 1.0000000 | NA | NA |
6.3.3.1.3 Phylogenetic
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.01334 0.013340 0.6524 999 0.435
Residuals 52 1.06332 0.020449
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
0_Wild 1_Acclimation
0_Wild 0.437
1_Acclimation 0.42294
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| time_point | 1 | 0.2890434 | 0.0766494 | 7.532050 | 0.001 |
| species | 1 | 0.3508889 | 0.0930498 | 9.143655 | 0.001 |
| individual | 25 | 2.1332925 | 0.5657133 | 2.223620 | 0.001 |
| Residual | 26 | 0.9977533 | 0.2645874 | NA | NA |
| Total | 53 | 3.7709782 | 1.0000000 | NA | NA |
6.3.3.1.4 Functional
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.0123 0.012300 0.4817 999 0.482
Residuals 52 1.3277 0.025533
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
0_Wild 1_Acclimation
0_Wild 0.487
1_Acclimation 0.49073
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| time_point | 1 | 0.0448774 | 0.0269021 | 2.355512 | 0.163 |
| species | 1 | 0.0973005 | 0.0583275 | 5.107077 | 0.034 |
| individual | 25 | 1.0306426 | 0.6178264 | 2.163841 | 0.055 |
| Residual | 26 | 0.4953546 | 0.2969440 | NA | NA |
| Total | 53 | 1.6681751 | 1.0000000 | NA | NA |
beta_richness_nmds_accli1 <- beta_div_richness_accli1$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(accli1_nmds, by = c("sample" = "Tube_code"))
beta_neutral_nmds_accli1 <- beta_div_neutral_accli1$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(accli1_nmds, by = c("sample" = "Tube_code"))
beta_phylo_nmds_accli1 <- beta_div_phylo_accli1$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(accli1_nmds, by = join_by(sample == Tube_code))
beta_func_nmds_accli1 <- beta_div_func_accli1$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(accli1_nmds, by = join_by(sample == Tube_code))6.3.4 4. Do the antibiotics work?
6.3.4.1 Acclimation vs antibiotics
treat <- meta %>%
filter(time_point == "1_Acclimation" | time_point == "2_Antibiotics")
temp_genome_counts <- transform(genome_counts_filt, row.names = genome_counts_filt$genome)
temp_genome_counts$genome <- NULL
treat.counts <- temp_genome_counts[,which(colnames(temp_genome_counts) %in% rownames(treat))]
identical(sort(colnames(treat.counts)),sort(as.character(rownames(treat))))
treat_nmds <- sample_metadata %>%
filter(time_point == "1_Acclimation" | time_point == "2_Antibiotics")6.3.4.2 Number of samples used
[1] 50
beta_div_richness_treat<-hillpair(data=treat.counts, q=0)
beta_div_neutral_treat<-hillpair(data=treat.counts, q=1)
beta_div_phylo_treat<-hillpair(data=treat.counts, q=1, tree=genome_tree)
beta_div_func_treat<-hillpair(data=treat.counts, q=1, dist=dist)6.3.4.2.1 Richness
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.025318 0.0253178 6.021 999 0.023 *
Residuals 48 0.201837 0.0042049
---
Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
1_Acclimation 2_Antibiotics
1_Acclimation 0.027
2_Antibiotics 0.017817
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| time_point | 1 | 1.888584 | 0.0949462 | 6.361098 | 0.001 |
| species | 1 | 2.117109 | 0.1064350 | 7.130814 | 0.001 |
| individual | 25 | 9.353701 | 0.4702455 | 1.260199 | 0.005 |
| Residual | 22 | 6.531709 | 0.3283734 | NA | NA |
| Total | 49 | 19.891103 | 1.0000000 | NA | NA |
6.3.4.2.2 Neutral
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.039587 0.039587 6.8387 999 0.013 *
Residuals 48 0.277854 0.005789
---
Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
1_Acclimation 2_Antibiotics
1_Acclimation 0.015
2_Antibiotics 0.011886
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| time_point | 1 | 2.024181 | 0.1063620 | 9.051981 | 0.001 |
| species | 1 | 2.853103 | 0.1499183 | 12.758858 | 0.001 |
| individual | 25 | 9.234189 | 0.4852168 | 1.651783 | 0.001 |
| Residual | 22 | 4.919584 | 0.2585029 | NA | NA |
| Total | 49 | 19.031057 | 1.0000000 | NA | NA |
6.3.4.2.3 Phylogenetic
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.58372 0.58372 35.413 999 0.001 ***
Residuals 48 0.79119 0.01648
---
Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
1_Acclimation 2_Antibiotics
1_Acclimation 0.001
2_Antibiotics 2.9795e-07
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| time_point | 1 | 1.8065206 | 0.2113909 | 18.636551 | 0.001 |
| species | 1 | 0.7903334 | 0.0924813 | 8.153292 | 0.001 |
| individual | 25 | 3.8164689 | 0.4465860 | 1.574869 | 0.005 |
| Residual | 22 | 2.1325541 | 0.2495419 | NA | NA |
| Total | 49 | 8.5458771 | 1.0000000 | NA | NA |
6.3.4.2.4 Functional
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 1 0.18591 0.185914 5.0679 999 0.023 *
Residuals 48 1.76088 0.036685
---
Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
1_Acclimation 2_Antibiotics
1_Acclimation 0.032
2_Antibiotics 0.028989
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| time_point | 1 | 1.8020952 | 0.3750193 | 33.6195614 | 0.001 |
| species | 1 | 0.0031247 | 0.0006503 | 0.0582938 | 0.848 |
| individual | 25 | 1.8208629 | 0.3789249 | 1.3587875 | 0.222 |
| Residual | 22 | 1.1792568 | 0.2454055 | NA | NA |
| Total | 49 | 4.8053396 | 1.0000000 | NA | NA |
beta_richness_nmds_treat <- beta_div_richness_treat$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(treat_nmds, by = c("sample" = "Tube_code"))
beta_neutral_nmds_treat <- beta_div_neutral_treat$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(treat_nmds, by = c("sample" = "Tube_code"))
beta_phylo_nmds_treat <- beta_div_phylo_treat$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(treat_nmds, by = join_by(sample == Tube_code))
beta_func_nmds_treat <- beta_div_func_treat$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(treat_nmds, by = join_by(sample == Tube_code))6.3.5 5. Does the FMT work?
6.3.5.1 Comparison between FMT2 vs Post-FMT2
#Create newID to identify duplicated samples
transplants_metadata<-sample_metadata%>%
mutate(Tube_code=str_remove_all(Tube_code, "_a"))
transplants_metadata$newID <- paste(transplants_metadata$Tube_code, "_", transplants_metadata$individual)
transplant3<-transplants_metadata%>%
filter(time_point == "4_Transplant2" | time_point == "6_Post-FMT2")%>%
column_to_rownames("newID")
transplant3_nmds <- transplants_metadata %>%
filter(time_point == "4_Transplant2" | time_point == "6_Post-FMT2")
full_counts<-temp_genome_counts %>%
t()%>%
as.data.frame()%>%
rownames_to_column("Tube_code")%>%
full_join(transplants_metadata,by = join_by(Tube_code == Tube_code))
transplant3_counts<-full_counts %>%
filter(time_point == "4_Transplant2" | time_point == "6_Post-FMT2") %>%
subset(select=-c(315:324)) %>%
column_to_rownames("newID")%>%
subset(select=-c(1))%>%
t() %>%
as.data.frame() %>%
mutate_if(is.character, as.numeric)
identical(sort(colnames(transplant3_counts)),sort(as.character(rownames(transplant3))))6.3.5.2 Number of samples used
[1] 49
beta_div_richness_transplant3<-hillpair(data=transplant3_counts, q=0)
beta_div_neutral_transplant3<-hillpair(data=transplant3_counts, q=1)
beta_div_phylo_transplant3<-hillpair(data=transplant3_counts, q=1, tree=genome_tree)
beta_div_func_transplant3<-hillpair(data=transplant3_counts, q=1, dist=dist)
#Arrange of metadata dataframe
transplant3_arrange<-transplant3[labels(beta_div_neutral_transplant3$S),]6.3.5.2.1 Richness
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 1.180473 | 0.0855095 | 6.984555 | 0.001 |
| time_point | 1 | 0.860906 | 0.0623612 | 5.093759 | 0.001 |
| type | 1 | 1.459433 | 0.1057165 | 8.635089 | 0.001 |
| individual | 24 | 6.755100 | 0.4893170 | 1.665341 | 0.001 |
| Residual | 21 | 3.549250 | 0.2570959 | NA | NA |
| Total | 48 | 13.805162 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Control vs Treatment 1 1.4169018 5.739828 0.15622903 0.001 0.003 *
2 Control vs Hot_control 1 2.0940966 8.509112 0.21005427 0.001 0.003 *
3 Treatment vs Hot_control 1 0.3004618 1.265034 0.04179854 0.159 0.477
6.3.5.2.2 Neutral
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 1.2800927 | 0.0939787 | 8.796453 | 0.001 |
| time_point | 1 | 0.9350566 | 0.0686477 | 6.425458 | 0.001 |
| type | 1 | 1.9135997 | 0.1404879 | 13.149743 | 0.001 |
| individual | 24 | 6.4363516 | 0.4725281 | 1.842870 | 0.001 |
| Residual | 21 | 3.0559984 | 0.2243577 | NA | NA |
| Total | 48 | 13.6210990 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Control vs Treatment 1 1.8758788 8.282671 0.21084796 0.001 0.003 *
2 Control vs Hot_control 1 2.4396317 10.635546 0.24945256 0.001 0.003 *
3 Treatment vs Hot_control 1 0.3158428 1.394345 0.04587515 0.126 0.378
6.3.5.2.3 Phylogenetic
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 0.1400466 | 0.0952654 | 6.956436 | 0.002 |
| time_point | 1 | 0.1138047 | 0.0774145 | 5.652939 | 0.001 |
| type | 1 | 0.1432667 | 0.0974558 | 7.116383 | 0.001 |
| individual | 24 | 0.6501795 | 0.4422784 | 1.345663 | 0.041 |
| Residual | 21 | 0.4227709 | 0.2875859 | NA | NA |
| Total | 48 | 1.4700683 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Control vs Treatment 1 0.14387705 5.735321 0.15612552 0.001 0.003 *
2 Control vs Hot_control 1 0.22715701 9.044894 0.22036587 0.001 0.003 *
3 Treatment vs Hot_control 1 0.04648319 1.704277 0.05550617 0.129 0.387
6.3.5.2.4 Functional
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 0.0092808 | 0.0077189 | 0.4182529 | 0.493 |
| time_point | 1 | -0.0061674 | -0.0051295 | -0.2779456 | 0.895 |
| type | 1 | 0.0831052 | 0.0691191 | 3.7452726 | 0.093 |
| individual | 24 | 0.6501528 | 0.5407359 | 1.2208414 | 0.345 |
| Residual | 21 | 0.4659767 | 0.3875556 | NA | NA |
| Total | 48 | 1.2023481 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Control vs Treatment 1 0.078539743 4.59293783 0.129040706 0.069 0.207
2 Control vs Hot_control 1 0.052468954 2.13675422 0.062593948 0.165 0.495
3 Treatment vs Hot_control 1 -0.002340352 -0.07432315 -0.002569452 0.887 1.000
beta_richness_nmds_transplant3 <- beta_div_richness_transplant3$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(transplant3_nmds, by = join_by(sample == newID))
beta_neutral_nmds_transplant3 <- beta_div_neutral_transplant3$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(transplant3_nmds, by = join_by(sample == newID))
beta_phylo_nmds_transplant3 <- beta_div_phylo_transplant3$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(transplant3_nmds, by = join_by(sample == newID))
beta_func_nmds_transplant3 <- beta_div_func_transplant3$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(transplant3_nmds, by = join_by(sample == newID))p0<-beta_richness_nmds_transplant3 %>%
group_by(individual) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type, shape=time_point)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y = "NMDS2", x="NMDS1 \n Richness beta diversity") +
theme_classic() +
theme(legend.position="none")
p1<-beta_neutral_nmds_transplant3 %>%
group_by(individual) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type, shape=time_point)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y = "NMDS2", x="NMDS1 \n Neutral beta diversity") +
theme_classic() +
theme(legend.position="none")
p2<-beta_phylo_nmds_transplant3 %>%
group_by(individual) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type, shape=time_point)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y= element_blank (), x="NMDS1 \n Phylogenetic beta diversity") +
theme_classic() +
theme(legend.position="none")
p3<-beta_func_nmds_transplant3 %>%
group_by(individual) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type, shape=time_point)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y= element_blank (), x="NMDS1 \n Functional beta diversity") +
theme_classic()+
theme(legend.position="none")6.3.5.3 Comparison between the different experimental time points
6.3.5.3.1 Comparison against Wild samples
The estimated time for calculating the 2850 pairwise combinations is 14 seconds.
6.3.6 6. Are there differences between the control and the treatment group?
6.3.6.2 Number of samples used
[1] 26
beta_div_richness_post1<-hillpair(data=post1.counts, q=0)
beta_div_neutral_post1<-hillpair(data=post1.counts, q=1)
beta_div_phylo_post1<-hillpair(data=post1.counts, q=1, tree=genome_tree)
beta_div_func_post1<-hillpair(data=post1.counts, q=1, dist=dist)
#Arrange of metadata dataframe
post1_arrange<-post1[labels(beta_div_neutral_post1$S),]6.3.6.2.1 Richness
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 2 0.017675 0.0088373 2.3825 999 0.099 .
Residuals 23 0.085312 0.0037092
---
Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Control Hot_control Treatment
Control 0.0060000 0.661
Hot_control 0.0068795 0.212
Treatment 0.6248469 0.2084296
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 0.6340254 | 0.0768024 | 2.065607 | 0.004 |
| type | 1 | 0.5615418 | 0.0680222 | 1.829461 | 0.010 |
| Residual | 23 | 7.0597099 | 0.8551754 | NA | NA |
| Total | 25 | 8.2552771 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Control vs Treatment 1 0.5615418 1.729004 0.1033537 0.016 0.048 .
2 Control vs Hot_control 1 0.8438429 2.793772 0.1486541 0.002 0.006 *
3 Treatment vs Hot_control 1 0.3734921 1.268929 0.0779971 0.098 0.294
6.3.6.2.2 Neutral
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 2 0.011001 0.0055005 0.6303 999 0.564
Residuals 23 0.200714 0.0087267
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Control Hot_control Treatment
Control 0.21500 0.957
Hot_control 0.21166 0.467
Treatment 0.95468 0.43604
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 0.7907904 | 0.1076445 | 3.056657 | 0.001 |
| type | 1 | 0.6051778 | 0.0823784 | 2.339205 | 0.009 |
| Residual | 23 | 5.9503501 | 0.8099772 | NA | NA |
| Total | 25 | 7.3463184 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Control vs Treatment 1 0.6051778 2.250849 0.13047758 0.009 0.027 .
2 Control vs Hot_control 1 1.0528902 4.143637 0.20570451 0.001 0.003 *
3 Treatment vs Hot_control 1 0.4150076 1.637268 0.09840968 0.046 0.138
6.3.6.2.3 Phylogenetic
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 2 0.00440 0.0021994 0.1369 999 0.91
Residuals 23 0.36941 0.0160614
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Control Hot_control Treatment
Control 0.92400 0.694
Hot_control 0.91505 0.803
Treatment 0.63312 0.73046
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 0.0560850 | 0.0531376 | 1.3149967 | 0.280 |
| type | 1 | 0.0184254 | 0.0174571 | 0.4320099 | 0.791 |
| Residual | 23 | 0.9809570 | 0.9294053 | NA | NA |
| Total | 25 | 1.0554673 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Control vs Treatment 1 0.01842535 0.4144162 0.02688498 0.775 1.000
2 Control vs Hot_control 1 0.05987967 1.7387847 0.09802164 0.117 0.351
3 Treatment vs Hot_control 1 0.03212966 0.6477782 0.04139746 0.692 1.000
6.3.6.2.4 Functional
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 2 0.00400 0.0020014 0.145 999 0.864
Residuals 23 0.31753 0.0138057
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Control Hot_control Treatment
Control 0.59900 0.750
Hot_control 0.59817 0.849
Treatment 0.75141 0.83718
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| species | 1 | 0.0024979 | 0.0033024 | 0.0900845 | 0.638 |
| type | 1 | 0.1161466 | 0.1535542 | 4.1887855 | 0.063 |
| Residual | 23 | 0.6377435 | 0.8431434 | NA | NA |
| Total | 25 | 0.7563879 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Control vs Treatment 1 0.11614656 4.724791 0.23953568 0.069 0.207
2 Control vs Hot_control 1 0.05000930 1.704826 0.09629160 0.224 0.672
3 Treatment vs Hot_control 1 0.01235859 0.423812 0.02747777 0.503 1.000
beta_richness_nmds_post1 <- beta_div_richness_post1$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(post1_nmds, by = join_by(sample == Tube_code))
beta_neutral_nmds_post1 <- beta_div_neutral_post1$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(post1_nmds, by = join_by(sample == Tube_code))
beta_phylogenetic_nmds_post1 <- beta_div_phylo_post1$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(post1_nmds, by = join_by(sample == Tube_code))
beta_functional_nmds_post1 <- beta_div_func_post1$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(post1_nmds, by = join_by(sample == Tube_code))p0<-beta_richness_nmds_post1 %>%
group_by(type) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y = "NMDS2", x="NMDS1 \n Richness beta diversity") +
theme_classic() +
theme(legend.position="none")
p1<-beta_neutral_nmds_post1 %>%
group_by(type) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y = "NMDS2", x="NMDS1 \n Neutral beta diversity") +
theme_classic() +
theme(legend.position="none")
p2<-beta_phylogenetic_nmds_post1 %>%
group_by(type) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y= element_blank (), x="NMDS1 \n Phylogenetic beta diversity") +
theme_classic() +
theme(legend.position="none")
p3<-beta_functional_nmds_post1 %>%
group_by(type) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y= element_blank (), x="NMDS1 \n Functional beta diversity") +
theme_classic()+
theme(legend.position="none")6.3.6.4 Number of samples used
[1] 27
beta_div_richness_post2<-hillpair(data=post2.counts, q=0)
beta_div_neutral_post2<-hillpair(data=post2.counts, q=1)
beta_div_phylo_post2<-hillpair(data=post2.counts, q=1, tree=genome_tree)
beta_div_func_post2<-hillpair(data=post2.counts, q=1, dist=dist)
#Arrange of metadata dataframe
post2_arrange<-post2[labels(beta_div_neutral_post2$S),]6.3.6.4.1 Richness
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 2 0.002011 0.0010056 0.1982 999 0.83
Residuals 24 0.121775 0.0050740
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Control Hot_control Treatment
Control 0.70300 0.786
Hot_control 0.67789 0.624
Treatment 0.79246 0.59820
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| type | 2 | 1.504341 | 0.1967776 | 2.939822 | 0.001 |
| Residual | 24 | 6.140538 | 0.8032224 | NA | NA |
| Total | 26 | 7.644879 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Treatment vs Control 1 0.6463814 2.560441 0.1379515 0.001 0.003 *
2 Treatment vs Hot_control 1 0.4796256 1.916520 0.1069694 0.001 0.003 *
3 Control vs Hot_control 1 1.1305044 4.268317 0.2105906 0.001 0.003 *
6.3.6.4.2 Neutral
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 2 0.008262 0.0041311 0.8024 999 0.468
Residuals 24 0.123559 0.0051483
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Control Hot_control Treatment
Control 0.46700 0.694
Hot_control 0.44675 0.241
Treatment 0.65989 0.25095
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| type | 2 | 1.923807 | 0.2603795 | 4.224537 | 0.001 |
| Residual | 24 | 5.464666 | 0.7396205 | NA | NA |
| Total | 26 | 7.388473 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Treatment vs Control 1 1.0227481 4.648335 0.2251191 0.001 0.003 *
2 Treatment vs Hot_control 1 0.5010202 2.206532 0.1211945 0.001 0.003 *
3 Control vs Hot_control 1 1.3619424 5.771031 0.2650785 0.001 0.003 *
6.3.6.4.3 Phylogenetic
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 2 0.000407 0.0002034 0.0487 999 0.959
Residuals 24 0.100305 0.0041794
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Control Hot_control Treatment
Control 0.92800 0.874
Hot_control 0.93765 0.769
Treatment 0.83933 0.76015
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| type | 2 | 0.1594363 | 0.2042241 | 3.079623 | 0.001 |
| Residual | 24 | 0.6212564 | 0.7957759 | NA | NA |
| Total | 26 | 0.7806927 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Treatment vs Control 1 0.05927454 2.382025 0.1295845 0.021 0.063
2 Treatment vs Hot_control 1 0.06906280 2.722460 0.1454115 0.005 0.015 .
3 Control vs Hot_control 1 0.11081709 4.043656 0.2017424 0.001 0.003 *
6.3.6.4.4 Functional
Permutation test for homogeneity of multivariate dispersions
Permutation: free
Number of permutations: 999
Response: Distances
Df Sum Sq Mean Sq F N.Perm Pr(>F)
Groups 2 0.01126 0.0056302 0.2861 999 0.773
Residuals 24 0.47233 0.0196806
Pairwise comparisons:
(Observed p-value below diagonal, permuted p-value above diagonal)
Control Hot_control Treatment
Control 0.54800 0.634
Hot_control 0.48255 0.790
Treatment 0.60116 0.75643
| Df | SumOfSqs | R2 | F | Pr(>F) | |
|---|---|---|---|---|---|
| type | 2 | -0.0038724 | -0.0056213 | -0.0670788 | 0.936 |
| Residual | 24 | 0.6927468 | 1.0056213 | NA | NA |
| Total | 26 | 0.6888744 | 1.0000000 | NA | NA |
pairs Df SumsOfSqs F.Model R2 p.value p.adjusted sig
1 Treatment vs Control 1 -0.008527330 -0.46290555 -0.029793572 0.853 1
2 Treatment vs Hot_control 1 -0.001648721 -0.04717131 -0.002956924 0.910 1
3 Control vs Hot_control 1 0.004367477 0.13147026 0.008149924 0.690 1
beta_richness_nmds_post2 <- beta_div_richness_post2$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(post2_nmds, by = join_by(sample == Tube_code))
beta_neutral_nmds_post2 <- beta_div_neutral_post2$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(post2_nmds, by = join_by(sample == Tube_code))
beta_phylogenetic_nmds_post2 <- beta_div_phylo_post2$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(post2_nmds, by = join_by(sample == Tube_code))
beta_functional_nmds_post2 <- beta_div_func_post2$S %>%
metaMDS(.,trymax = 500, k=2, verbosity=FALSE) %>%
scores() %>%
as_tibble(., rownames = "sample") %>%
left_join(post2_nmds, by = join_by(sample == Tube_code))p0<-beta_richness_nmds_post2 %>%
group_by(type) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y = "NMDS2", x="NMDS1 \n Richness beta diversity") +
theme_classic() +
theme(legend.position="none")
p1<-beta_neutral_nmds_post2 %>%
group_by(type) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y = "NMDS2", x="NMDS1 \n Neutral beta diversity") +
theme_classic() +
theme(legend.position="none")
p2<-beta_phylogenetic_nmds_post2 %>%
group_by(type) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y= element_blank (), x="NMDS1 \n Phylogenetic beta diversity") +
theme_classic() +
theme(legend.position="none")
p3<-beta_functional_nmds_post2 %>%
group_by(type) %>%
mutate(x_cen = mean(NMDS1, na.rm = TRUE)) %>%
mutate(y_cen = mean(NMDS2, na.rm = TRUE)) %>%
ungroup() %>%
ggplot(., aes(x=NMDS1,y=NMDS2, color=type)) +
scale_color_manual(name="Type",
breaks=c("Control", "Hot_control", "Treatment"),
labels=c("Cold-Cold", "Hot-Hot", "Cold-Hot"),
values=c("#4477AA","#d57d2c","#76b183")) +
geom_point(size=2) +
geom_segment(aes(x=x_cen, y=y_cen, xend=NMDS1, yend=NMDS2), alpha=0.2) +
labs(y= element_blank (), x="NMDS1 \n Functional beta diversity") +
theme_classic()+
theme(legend.position="none")